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Langerhans cell histiocytosis

Langerhans cell histiocytosis (LCH) is a systemic disease associated with the proliferation and accumulation (usually in granulomas) of Langerhans cells in various tissues.

Fulminant hepatitis

Acute hepatitis complicated by acute liver failure with hepatic encephalopathy occurring less than 8 weeks after the onset of jaundice.

合計: 1

（表示件数）

PMID (PMCID)
16237711	FEMALE	Infant
	Langerhans' cell histiocytosis after living donor liver transplantation: report of a case.
	Honda R, Ohno Y, Iwasaki T, Okudaira S, Okada M, Kamitamari A, Ohshima K, Moriuchi H, Kanematsu T. Liver Transpl. 2005;11(11):1435-8.
	We report a case of Langerhans' cell histiocytosis (LCH) occurring after a living donor liver transplantation (LDLT) for fulminant hepatitis.